Canonical Allele Identifier: PA2826297919
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2500184
ClinVar RCV Id: RCV004548501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229305.1:p.Gly18Val
CA399849182
NM_001242376.3:c.53G>T